GB/T 18268.26-2010
ActiveElectrical equipment for measurement, control and laboratory use - EMC requirements - Part 26: Particular requirements - In vitro diagnostic (IVD) medical equipment
测量、控制和实验室用的电设备 电磁兼容性要求 第26部分：特殊要求 体外诊断(IVD)医疗设备
Application Summary AI generated
This standard specifies electromagnetic compatibility (EMC) immunity and emission requirements specifically for in vitro diagnostic (IVD) medical equipment used in clinical laboratories or point-of-care settings. It applies to electrical devices that analyze human samples (e.g., blood, urine) for diagnosis, ensuring they do not interfere with other equipment or malfunction due to electromagnetic disturbances. Manufacturers and test laboratories use this standard to verify compliance with Chinese EMC regulations for IVD devices before market release.
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Transparency note: The application summary and key sentences on this page were automatically generated by AI from the standard's original text. This content has not been human-verified and should not be used for compliance or regulatory purposes. Always refer to the official standard document from the issuing authority.